BRPI0917808A2 - cmet inhibitors - Google Patents
cmet inhibitorsInfo
- Publication number
- BRPI0917808A2 BRPI0917808A2 BRPI0917808A BRPI0917808A BRPI0917808A2 BR PI0917808 A2 BRPI0917808 A2 BR PI0917808A2 BR PI0917808 A BRPI0917808 A BR PI0917808A BR PI0917808 A BRPI0917808 A BR PI0917808A BR PI0917808 A2 BRPI0917808 A2 BR PI0917808A2
- Authority
- BR
- Brazil
- Prior art keywords
- cmet inhibitors
- cmet
- inhibitors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8895908P | 2008-08-14 | 2008-08-14 | |
US11791008P | 2008-11-25 | 2008-11-25 | |
US16100709P | 2009-03-17 | 2009-03-17 | |
PCT/US2009/053913 WO2010019899A1 (en) | 2008-08-14 | 2009-08-14 | cMET INHIBITORS |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0917808A2 true BRPI0917808A2 (en) | 2019-09-24 |
Family
ID=41202532
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0917808A BRPI0917808A2 (en) | 2008-08-14 | 2009-08-14 | cmet inhibitors |
Country Status (26)
Country | Link |
---|---|
US (1) | US8178534B2 (en) |
EP (1) | EP2313407B1 (en) |
JP (1) | JP5469666B2 (en) |
KR (1) | KR20110039383A (en) |
CN (1) | CN102124005B (en) |
AR (1) | AR072936A1 (en) |
AU (1) | AU2009281822B2 (en) |
BR (1) | BRPI0917808A2 (en) |
CA (1) | CA2731108A1 (en) |
CO (1) | CO6351724A2 (en) |
CR (1) | CR20110135A (en) |
DO (1) | DOP2011000050A (en) |
EA (1) | EA019723B1 (en) |
EC (1) | ECSP11010889A (en) |
ES (1) | ES2608761T3 (en) |
GE (1) | GEP20125652B (en) |
IL (1) | IL210734A0 (en) |
MA (1) | MA32615B1 (en) |
MX (1) | MX2011001732A (en) |
MY (1) | MY150542A (en) |
NZ (1) | NZ590617A (en) |
PE (1) | PE20110275A1 (en) |
TW (1) | TWI455939B (en) |
UY (1) | UY32049A (en) |
WO (1) | WO2010019899A1 (en) |
ZA (1) | ZA201100467B (en) |
Families Citing this family (79)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR059898A1 (en) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | DERIVATIVES OF 3-CIANO-PIRIDONA 1,4-DISUSTITUTED AND ITS USE AS ALLOSTERIC MODULATORS OF MGLUR2 RECEIVERS |
TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
US20090197880A1 (en) * | 2007-07-13 | 2009-08-06 | Genelabs Technologies, Inc. | Anti-viral compounds, compositions, and methods of use |
CN101801930B (en) | 2007-09-14 | 2013-01-30 | 奥梅-杨森制药有限公司 | 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones |
AU2008297876B2 (en) | 2007-09-14 | 2011-07-07 | Addex Pharma S.A. | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
BRPI0816767B8 (en) | 2007-09-14 | 2021-05-25 | Addex Pharmaceuticals Sa | compound 4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-disubstituted 1',3'-ones, pharmaceutical composition and use of same |
ES2637794T3 (en) | 2007-11-14 | 2017-10-17 | Janssen Pharmaceuticals, Inc. | Imidazo [1,2-A] pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors |
JPWO2009128520A1 (en) * | 2008-04-18 | 2011-08-04 | 塩野義製薬株式会社 | Heterocyclic compounds having PI3K inhibitory activity |
AU2009289784B2 (en) | 2008-09-02 | 2012-03-22 | Addex Pharma S.A. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
WO2010043396A1 (en) | 2008-10-16 | 2010-04-22 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
WO2010060589A1 (en) | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
US8946205B2 (en) | 2009-05-12 | 2015-02-03 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
MY161325A (en) | 2009-05-12 | 2017-04-14 | Janssen Pharmaceuticals Inc | 1, 2, 4-triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
EP2343294A1 (en) | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Substituted triazolopyridines |
PL2719699T3 (en) | 2009-12-31 | 2016-01-29 | Hutchison Medipharma Ltd | Certain triazolopyrazines, compositions thereof and methods of use therefor |
WO2011145035A1 (en) | 2010-05-17 | 2011-11-24 | Indian Incozen Therapeutics Pvt. Ltd. | Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of protein kinases |
WO2012003338A1 (en) * | 2010-07-01 | 2012-01-05 | Takeda Pharmaceutical Company Limited | COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET |
CN103261195B (en) | 2010-11-08 | 2015-09-02 | 杨森制药公司 | The purposes of 1,2,4-triazolo [4,3-a] pyridine derivate and the positive allosteric modulators as MGLUR2 acceptor thereof |
AU2011328203B2 (en) | 2010-11-08 | 2015-03-19 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
PL2649069T3 (en) | 2010-11-08 | 2016-01-29 | Janssen Pharmaceuticals Inc | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
UY34329A (en) * | 2011-09-15 | 2013-04-30 | Novartis Ag | TRIAZOLOPIRIDINE COMPOUNDS |
CN103958509B (en) * | 2011-09-15 | 2015-12-23 | 诺华股份有限公司 | As 3-(quinoline-6-base sulfo-)-[1,2,4] triazolo [4,3-A] pyridine compounds that the 6-of tyrosine kinase inhibitor replaces |
CN103030654A (en) * | 2011-10-09 | 2013-04-10 | 济南赛文医药技术有限公司 | Micromolecular c-Met protein kinase inhibitor |
WO2013135674A1 (en) * | 2012-03-12 | 2013-09-19 | Syngenta Participations Ag | Insecticidal 2-aryl-acetamide compounds |
ES2704744T3 (en) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Substituted tricyclic compounds as FGFR inhibitors |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
CN109776525B (en) | 2013-04-19 | 2022-01-21 | 因赛特控股公司 | Bicyclic heterocycles as FGFR inhibitors |
JP6355719B2 (en) * | 2013-05-10 | 2018-07-11 | ジエンス ハンセン ファーマセウティカル カンパニー リミテッド | [1,2,4] Triazole [4,3-a] pyridine derivative, production method thereof or pharmaceutical application thereof |
JO3368B1 (en) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
EP2818471A1 (en) * | 2013-06-27 | 2014-12-31 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5 |
JO3367B1 (en) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
KR102461134B1 (en) | 2014-01-21 | 2022-10-28 | 얀센 파마슈티카 엔.브이. | Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use |
UA121965C2 (en) | 2014-01-21 | 2020-08-25 | Янссен Фармацевтика Нв | Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use |
US9670210B2 (en) | 2014-02-13 | 2017-06-06 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
WO2015123437A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
EP3392244A1 (en) | 2014-02-13 | 2018-10-24 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
TWI720451B (en) | 2014-02-13 | 2021-03-01 | 美商英塞特控股公司 | Cyclopropylamines as lsd1 inhibitors |
US9695167B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors |
TWI687419B (en) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | Imidazopyridines and imidazopyrazines as LSD1 inhibitors |
US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
WO2016007736A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyrazines as lsd1 inhibitors |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MA41551A (en) | 2015-02-20 | 2017-12-26 | Incyte Corp | BICYCLIC HETEROCYCLES USED AS FGFR4 INHIBITORS |
AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
EA201792205A1 (en) | 2015-04-03 | 2018-02-28 | Инсайт Корпорейшн | HETEROCYCLIC COMPOUNDS AS LSD1 INHIBITORS |
ES2928684T3 (en) * | 2015-06-25 | 2022-11-21 | Taiho Pharmaceutical Co Ltd | Therapeutic agent for fibrosis |
AU2016306555B2 (en) | 2015-08-12 | 2021-01-28 | Incyte Holdings Corporation | Salts of an LSD1 inhibitor |
CN108853108A (en) * | 2015-12-31 | 2018-11-23 | 北京浦润奥生物科技有限责任公司 | Compound is preparing the purposes in the drug for treating glioma |
JP6974331B2 (en) | 2016-02-05 | 2021-12-01 | デナリ セラピューティクス インコーポレイテッドDenali Therapeutics Inc. | Compounds, compositions and methods |
US10166221B2 (en) | 2016-04-22 | 2019-01-01 | Incyte Corporation | Formulations of an LSD1 inhibitor |
WO2018095953A1 (en) | 2016-11-23 | 2018-05-31 | Bayer Cropscience Aktiengesellschaft | 2-[3-(alkylsulfonyl)-2h-indazol-2-yl]-3h-imidazo[4,5-b]pyridine derivatives and similar compounds as pesticides |
HUE058802T2 (en) | 2016-12-09 | 2022-09-28 | Denali Therapeutics Inc | Compounds useful as ripk1 inhibitors |
CN110312511B (en) | 2017-02-15 | 2023-10-27 | 大鹏药品工业株式会社 | Pharmaceutical composition |
AR111960A1 (en) | 2017-05-26 | 2019-09-04 | Incyte Corp | CRYSTALLINE FORMS OF A FGFR INHIBITOR AND PROCESSES FOR ITS PREPARATION |
MX2020011639A (en) | 2018-05-04 | 2021-02-15 | Incyte Corp | Salts of an fgfr inhibitor. |
BR112020022392A2 (en) | 2018-05-04 | 2021-02-02 | Incyte Corporation | solid forms of a fgfr inhibitor and processes for preparing them |
WO2020047198A1 (en) | 2018-08-31 | 2020-03-05 | Incyte Corporation | Salts of an lsd1 inhibitor and processes for preparing the same |
US11161838B2 (en) | 2018-11-13 | 2021-11-02 | Incyte Corporation | Heterocyclic derivatives as PI3K inhibitors |
WO2020102216A1 (en) | 2018-11-13 | 2020-05-22 | Incyte Corporation | Substituted heterocyclic derivatives as pi3k inhibitors |
US11078204B2 (en) | 2018-11-13 | 2021-08-03 | Incyte Corporation | Heterocyclic derivatives as PI3K inhibitors |
MX2021006982A (en) | 2018-12-14 | 2021-09-10 | Beta Pharma Inc | Organophosphorus-substituted compounds as c-met inhibitors and therapeutic uses thereof. |
WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
EP3942045A1 (en) | 2019-03-21 | 2022-01-26 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
IL291901A (en) | 2019-10-14 | 2022-06-01 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
EP4054579A1 (en) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
KR20220131900A (en) | 2019-12-04 | 2022-09-29 | 인사이트 코포레이션 | Derivatives of FGFR inhibitors |
WO2021113479A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
EP4352059A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
AU2023206890A1 (en) | 2022-01-12 | 2024-08-22 | Denali Therapeutics Inc. | Crystalline forms of (s)-5-benzyl-n-(5-methyl-4-oxo-2, 3,4,5- tetrahydropyrido [3,2-b] [l,4]oxazepin-3-yl)-4h-l,2,4-triazole-3-carboxamide |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8719368D0 (en) * | 1987-08-15 | 1987-09-23 | Wellcome Found | Heterocyclic compounds |
US20070078136A1 (en) | 2005-09-22 | 2007-04-05 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
US7723336B2 (en) * | 2005-09-22 | 2010-05-25 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
AU2006320580B2 (en) | 2005-11-30 | 2011-06-23 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-Met and uses thereof |
ME02736B (en) * | 2005-12-21 | 2017-10-20 | Janssen Pharmaceutica Nv | Triazolopyridazines as tyrosine kinase modulators |
WO2008016192A2 (en) | 2006-08-04 | 2008-02-07 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivative and use thereof |
CA2660836A1 (en) * | 2006-08-07 | 2008-02-21 | Incyte Corporation | Triazolotriazines as kinase inhibitors |
EP1900739A1 (en) | 2006-08-30 | 2008-03-19 | Cellzome Ag | Diazolodiazine derivatives as kinase inhibitors |
WO2008030579A2 (en) | 2006-09-07 | 2008-03-13 | Biogen Idec Ma Inc. | Irak modulators for treating an inflammatory condition, cell proliferative disorder, immune disorder |
EP2084162B1 (en) | 2006-10-23 | 2012-09-12 | SGX Pharmaceuticals, Inc. | Bicyclic triazoles as protein kinase modulators |
EA026126B1 (en) | 2006-11-22 | 2017-03-31 | Инсайт Холдингс Корпорейшн | Imidazotriazines and imidazopyrimidines as kinase inhibitors |
PA8792501A1 (en) * | 2007-08-09 | 2009-04-23 | Sanofi Aventis | NEW DERIVATIVES OF 6-TRIAZOLOPIRIDACINA-SULFANIL BENZOTIAZOL AND BENCIMIDAZOL, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICATIONS, PHARMACEUTICAL COMPOSITIONS AND NEW MAIN USE AS MET INHIBITORS. |
MX2010009414A (en) | 2008-02-28 | 2010-09-24 | Novartis Ag | Imidazo [1,2-b] pyridazine derivatives for the treatment of c-met tyrosine kinase mediated disease. |
-
2009
- 2009-08-13 UY UY0001032049A patent/UY32049A/en not_active Application Discontinuation
- 2009-08-14 AU AU2009281822A patent/AU2009281822B2/en not_active Expired - Fee Related
- 2009-08-14 CN CN200980131456.9A patent/CN102124005B/en not_active Expired - Fee Related
- 2009-08-14 GE GEAP200912126A patent/GEP20125652B/en unknown
- 2009-08-14 PE PE2011000152A patent/PE20110275A1/en not_active Application Discontinuation
- 2009-08-14 MX MX2011001732A patent/MX2011001732A/en active IP Right Grant
- 2009-08-14 TW TW098127469A patent/TWI455939B/en not_active IP Right Cessation
- 2009-08-14 WO PCT/US2009/053913 patent/WO2010019899A1/en active Application Filing
- 2009-08-14 MY MYPI20110564 patent/MY150542A/en unknown
- 2009-08-14 AR ARP090103156A patent/AR072936A1/en unknown
- 2009-08-14 EP EP09791542.5A patent/EP2313407B1/en active Active
- 2009-08-14 JP JP2011523198A patent/JP5469666B2/en not_active Expired - Fee Related
- 2009-08-14 KR KR1020117005243A patent/KR20110039383A/en not_active Application Discontinuation
- 2009-08-14 CA CA2731108A patent/CA2731108A1/en not_active Abandoned
- 2009-08-14 BR BRPI0917808A patent/BRPI0917808A2/en not_active IP Right Cessation
- 2009-08-14 US US12/541,724 patent/US8178534B2/en not_active Expired - Fee Related
- 2009-08-14 ES ES09791542.5T patent/ES2608761T3/en active Active
- 2009-08-14 EA EA201170295A patent/EA019723B1/en not_active IP Right Cessation
- 2009-08-14 NZ NZ590617A patent/NZ590617A/en not_active IP Right Cessation
-
2011
- 2011-01-18 ZA ZA2011/00467A patent/ZA201100467B/en unknown
- 2011-01-18 IL IL210734A patent/IL210734A0/en unknown
- 2011-02-11 DO DO2011000050A patent/DOP2011000050A/en unknown
- 2011-03-07 MA MA33676A patent/MA32615B1/en unknown
- 2011-03-11 CO CO11030354A patent/CO6351724A2/en active IP Right Grant
- 2011-03-14 EC EC2011010889A patent/ECSP11010889A/en unknown
- 2011-03-14 CR CR20110135A patent/CR20110135A/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL210734A0 (en) | 2011-03-31 |
US8178534B2 (en) | 2012-05-15 |
EP2313407B1 (en) | 2016-10-05 |
CR20110135A (en) | 2011-09-27 |
WO2010019899A1 (en) | 2010-02-18 |
AR072936A1 (en) | 2010-09-29 |
JP2012500215A (en) | 2012-01-05 |
PE20110275A1 (en) | 2011-05-08 |
NZ590617A (en) | 2012-05-25 |
MY150542A (en) | 2014-01-30 |
MA32615B1 (en) | 2011-09-01 |
KR20110039383A (en) | 2011-04-15 |
GEP20125652B (en) | 2012-09-25 |
TW201014857A (en) | 2010-04-16 |
DOP2011000050A (en) | 2011-03-15 |
ECSP11010889A (en) | 2011-04-29 |
JP5469666B2 (en) | 2014-04-16 |
EA019723B1 (en) | 2014-05-30 |
TWI455939B (en) | 2014-10-11 |
UY32049A (en) | 2010-03-26 |
MX2011001732A (en) | 2011-03-25 |
ES2608761T3 (en) | 2017-04-12 |
EP2313407A1 (en) | 2011-04-27 |
CN102124005B (en) | 2014-06-04 |
ZA201100467B (en) | 2012-03-28 |
US20100063054A1 (en) | 2010-03-11 |
EA201170295A1 (en) | 2011-08-30 |
CN102124005A (en) | 2011-07-13 |
CO6351724A2 (en) | 2011-12-20 |
CA2731108A1 (en) | 2010-02-18 |
AU2009281822B2 (en) | 2014-11-13 |
AU2009281822A1 (en) | 2010-02-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY2020024I2 (en) | BETA-LACTAMAS INHIBITORS | |
BRPI0917808A2 (en) | cmet inhibitors | |
BRPI0911989A2 (en) | mycelic unions | |
BRPI0907376A2 (en) | Photobiorretador | |
DE602009000234D1 (en) | msignals | |
BRPI0914649A2 (en) | Piprazole-quinazolines | |
DE602008003521D1 (en) | Sitzrücklehnungsmechanismus | |
NL301273I2 (en) | vamorolone | |
BRPI0918564A2 (en) | inhibitors | |
BRPI0907522A2 (en) | biarlamides | |
BRPI0909634A2 (en) | 2-aminoquinolines | |
DE112009000183A5 (en) | Sicherheitsvorreiber | |
DK2240506T3 (en) | IAP inhibitors | |
DE112009001946A5 (en) | MOBELAUSZUGSFÜHRUNG | |
DE602009000488D1 (en) | Obstvereinzelvorrichtung | |
BRPI0907863A2 (en) | pyrrolopyrimidinecarboxamides | |
BRPI0909637A2 (en) | 2-aminoquinolines | |
DE602009000862D1 (en) | Gehwagenbremse | |
AT507449A3 (en) | DÄMMSTOFFBEFESTIGER | |
DE602009001190D1 (en) | Gleichstromumrichtervorrichtung | |
BRPI0918966A2 (en) | protease inhibitors | |
DE502008003019D1 (en) | Einschraubverschraubung | |
BRPI0919073A2 (en) | protease inhibitors | |
DE102008019532B8 (en) | Ölvormischbrenner | |
DE602009001033D1 (en) | Vorauflader |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] | ||
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2543 DE 01-10-2019 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |